Comparison of Core Stability, Body Awareness, Pelvic Health, Sleep, and Quality of Life in Physically Active Women With and Without Polyendocrine Metabolic Ovarian Syndrome
2026年8月5日 更新者：Ezgi Türkmen、Health Institutes of Turkey
Aim of the study was to compare physically active women with and without Polyendocrine Metabolic Ovarian Syndrome (PMOS) in terms of core stability, body awareness, pelvic health, sleep, and quality of life, and to reveal the possible effects of the presence of PMOS on these parameters despite physical activity.
研究概览
地位
招聘中
详细说明
The study plans to include female participants who have been regularly practicing Pilates at least twice a week for at least three months at a designated Pilates studio.
Data on participants' socio-demographic characteristics, core stability, body awareness, pelvic floor function, sleep, and quality of life will be collected.
This research study is designed as an observational and cross-sectional evaluation study.
研究类型
观察性的
注册 (估计的)
50
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习联系方式
- 姓名：Ezgi Türkmen
- 电话号码：0090 216 547 26 00
- 邮箱：turkmnezgi@gmail.com
学习地点
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Istanbul、土耳其（türkiye）
- 招聘中
- Haliç Üniversitesi
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接触：
- Ayşenur Çetinkaya
- 电话号码：0090 212 924 24 44
- 邮箱：aysenurcetinkaya@halic.edu.tr
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参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
接受健康志愿者
不
取样方法
非概率样本
研究人群
Participants with Polyendocrine Metabolic Ovarian Syndrome & Healthy Adults
描述
Inclusion Criteria:
- Being a woman aged 18-40 with a diagnosis of PMOS (n=25).
- Being a healthy woman aged 18-40 (n=25).
- Having practiced Pilates regularly for at least three months, at least twice a week.
- Voluntarily agreeing to participate in the study.
Exclusion Criteria:
- Being pregnant or in the first 6 months postpartum.
- Being in menopause.
- Having any other diagnosed gynecological pathology.
- Having any significant physical limitations that would prevent the tests from being performed.
- Having any diagnosed psychological disorder that would hinder communication.
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
队列和干预
团体/队列 |
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Group I
Paricipants with Polyendocrine Metabolic Ovarian Syndrome
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Group II
Healthy Adult Participants
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研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Forearm Plank Test
大体时间：Baseline
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The purpose of this test is to measure the core stability, or endurance, of the trunk muscles.
Participants are asked to keep their body in a straight line against gravity with their forearms on the ground and their toes touching the ground, and to maintain their posture without changing position by contracting their abdominal muscles.
The time (in seconds) spent in this position is measured and recorded with a stopwatch.
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Baseline
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Side Bridge Test
大体时间：Baseline
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The participant lies on their side with their elbow and forearm placed on the ground at shoulder level.
Legs and feet are placed on top of each other, forming a straight line.
The individual lifts their hips off the ground against gravity, bringing their body into a side bridge position parallel to the ground.
Both sides (right/left) are tested separately.
The time (in seconds) spent in this position is measured and recorded with a stopwatch.
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Baseline
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Body Awareness Questionnaire (BAQ)
大体时间：Baseline
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BAQ is an 18-item self-report scale designed to measure how attentive the participants are to normal, non-emotional internal bodily processes.
It evaluates the sensitivity to everyday bodily cycles (like sleep and hunger), ability to detect subtle changes, and capacity to anticipate physical reactions.
Typically takes about 3 to 5 minutes.
Items are generally rated on a 1 to 7 scale, with higher total scores indicating greater perceived condence and accuracy in monitoring the physical state over time.
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Baseline
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Pelvic Floor Distress Inventory-20 (PFDI-20)
大体时间：Baseline
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This scale, which assesses pelvic floor-related symptoms and pelvic functionality, consists of three subscales: POPDI-6, CRADI-8, and UDI-6.
The average of the responses for each subscale is calculated and multiplied by 25 to create a standard score on a scale of 0-100 for each subscale.
The total PFDI-20 score is obtained by summing the scores of the three subscales and ranges from 0 to 300.
Higher scores indicate more symptoms and discomfort.
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Baseline
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Pittsburgh Sleep Quality Index (PSQI)
大体时间：Baseline
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This scale was developed to assess sleep quality and disturbances over a one-month period.
The 18 items included in the scoring are grouped into 7 components.
Some components are represented by a single item, while others are obtained by combining several items.
Each item is rated on a scale of 0-3, and the scores of each component are added together to obtain a total score between 0-21.
A higher total score indicates poor sleep quality, while a score above 5 generally indicates poor sleep quality.
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Baseline
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WHO - Quality of Life - Brief (WHOQOL-BREF)
大体时间：Baseline
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The World Health Organization-developed quality of life assessment tool helps evaluate an individual's overall health status.
It consists of 26 questions, each scored on a 5-point Likert scale from 1 (very poor) to 5 (very good).
The scale covers four core areas of life: physical health, psychological health, social relationships, and environment.
It also includes two additional items that assess an individual's overall quality of life and health satisfaction.
Raw scores are converted into a total score on a scale of 0-100 using a formula.
Higher scores indicate a higher perceived quality of life.
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Baseline
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2026年8月5日
初级完成 (估计的)
2026年9月1日
研究完成 (估计的)
2026年9月1日
研究注册日期
首次提交
2026年7月27日
首先提交符合 QC 标准的
2026年7月30日
首次发布 (实际的)
2026年8月5日
研究记录更新
最后更新发布 (实际的)
2026年8月6日
上次提交的符合 QC 标准的更新
2026年8月5日
最后验证
2026年8月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.